IRF6 is a mediator of Notch pro-differentiation and tumour suppressive function in keratinocytes.
Data(s) |
2011
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Resumo |
While the pro-differentiation and tumour suppressive functions of Notch signalling in keratinocytes are well established, the underlying mechanisms remain poorly understood. We report here that interferon regulatory factor 6 (IRF6), an IRF family member with an essential role in epidermal development, is induced in differentiation through a Notch-dependent mechanism and is a primary Notch target in keratinocytes and keratinocyte-derived SCC cells. Increased IRF6 expression contributes to the impact of Notch activation on growth/differentiation-related genes, while it is not required for induction of 'canonical' Notch targets like p21(WAF1/Cip1), Hes1 and Hey1. Down-modulation of IRF6 counteracts differentiation of primary human keratinocytes in vitro and in vivo, promoting ras-induced tumour formation. The clinical relevance of these findings is illustrated by the strikingly opposite pattern of expression of Notch1 and IRF6 versus epidermal growth factor receptor in a cohort of clinical SCCs, as a function of their grade of differentiation. Thus, IRF6 is a primary Notch target in keratinocytes, which contributes to the role of this pathway in differentiation and tumour suppression. |
Identificador |
http://serval.unil.ch/?id=serval:BIB_6437DA9C05EF isbn:1460-2075 (Electronic) pmid:21909072 doi:10.1038/emboj.2011.325 isiid:000297691500006 |
Idioma(s) |
en |
Fonte |
Embo Journal, vol. 30, no. 22, pp. 4571-4585 |
Tipo |
info:eu-repo/semantics/article article |